Package 70010-073-44
Brand: potassium chloride
Generic: potassium chloridePackage Facts
Identity
Package NDC
70010-073-44
Digits Only
7001007344
Product NDC
70010-073
Description
473 mL in 1 BOTTLE (70010-073-44)
Marketing
Marketing Status
Brand
potassium chloride
Generic
potassium chloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "44f3fc8c-926c-1505-e063-6294a90a88fd", "openfda": {"upc": ["0370010073449", "0370010072442"], "unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["302b3fa7-ea87-4bf1-aae0-6a2d7459de86"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (70010-073-44)", "package_ndc": "70010-073-44", "marketing_start_date": "20210425"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "70010-073_44f3fc8c-926c-1505-e063-6294a90a88fd", "dosage_form": "SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "70010-073", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Granules Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "40 meq/15mL"}], "application_number": "ANDA213392", "marketing_category": "ANDA", "marketing_start_date": "20210425", "listing_expiration_date": "20261231"}